14 Records <strong>of</strong> <strong>the</strong> <strong>Australian</strong> Museum (2009) Vol. 61 Fig. 7. Paroistodus parallelus (P<strong>and</strong>er, 1856). All from sample WCB705/133. A–D, M element; (A), CPC39842, anterior view (IY117-002); B,C, CPC39843, (B), anterior view (IY117-005); (C), basal view (IY117-006); (D), CPC39844, posterior view (IY117-008). E–G, Sa element; E,F, CPC39845, (E), lateral view (IY117-010), (F), basal view (IY117-011); (G), CPC39846, lateral view (IY117-009). H–J, Sb element; (H), CPC39847, outer lateral view (IY117-017); I,J, CPC39848, (I), inner lateral view (IY117-016), (J), basal view (IY117-018). K–M, Sc element; K,L, CPC39849, (K), basal view (IY117-014), (L), inner lateral view (IY117-013); (M), CPC39850, outer lateral view (IY117-012). N,O, Sd element; (N), CPC39851, inner-basal view (IY117-025); (O), CPC39852, outer lateral view (IY117-029). (P), Pb element; CPC39853, outer lateral view (IY132-020). Q–S, ?Pa element, (Q), CPC39854, basal view (IY117-036), (R), CPC39855, outer lateral view (IY117-030); (S), CPC39856, inner lateral view (IY117-034). Scale bars 100 µm.
Material. 457 specimens from three samples (Table 1). Remarks. The species as revised by Löfgren (1997) possesses a septimembrate apparatus (including makellate M <strong>and</strong> drepanodiform or paroistodiform S <strong>and</strong> P elements), which can be distinguished from <strong>the</strong> o<strong>the</strong>r species <strong>of</strong> Paroistodus by having prominent lateral costae on <strong>the</strong> sides <strong>of</strong> its constituent elements. Zhen et al. (in press b) preferred to describe <strong>the</strong> S <strong>and</strong> P elements as paroistodiform in <strong>the</strong> Paroistodus species which show a sharp anterior costa extending basally into <strong>the</strong> basal cavity <strong>and</strong> forming a ridgelike structure (Zhen et al., 2007b, p. 137) at <strong>the</strong> anterior end <strong>of</strong> <strong>the</strong> basal cavity. However this character is not shown in <strong>the</strong> material <strong>of</strong> <strong>the</strong> two Paroistodus species (similar to Paroistodus sp. recently documented from <strong>the</strong> Honghuayuan Formation in South China) reported herein from <strong>the</strong> Emanuel Formation, although <strong>the</strong> anterior part <strong>of</strong> base <strong>of</strong>ten exhibits a zone <strong>of</strong> recessive basal margin (Figs 7A–C, 8H). Paroistodus parallelus occurs abundantly in <strong>the</strong> Emanuel Formation, where it is found in association with P. proteus although <strong>the</strong> latter is rare (Table 1). Paroistodus proteus (Lindström, 1955) emend. Löfgren, 1997 Fig. 8A–K Drepanodus proteus Lindström, 1955: 566, pl. 3, figs 18–21, text-fig. 2a–f, j. Paroistodus proteus (Lindström).—Löfgren, 1997: 922–923, text-figs 3H–N, 4L–AB (cum syn.); Zhen et al., 2007b: 136, 137, pl. 5, figs 1–11 (cum syn.). Material. 30 specimens from three samples (Table 1). Remarks. Paroistodus parallelus is relatively rare in <strong>the</strong> Emanuel samples, <strong>and</strong> can be easily differentiated from associated P. parallelus mainly by lacking a prominent costa on <strong>the</strong> lateral faces. Paroistodus proteus was revised by Löfgren (1997) as having a septimembrate apparatus. After a review <strong>of</strong> previously reported occurrences <strong>of</strong> this species in <strong>the</strong> Honghuayuan Formation <strong>and</strong> o<strong>the</strong>r coeval stratigraphic units in South China <strong>and</strong> comparison with Baltic material <strong>of</strong> P. proteus, Zhen et al. (2007b) concluded that Paroistodus is represented in <strong>the</strong> Honghuayuan Formation by a rare form that <strong>the</strong>y identified as Paroistodus sp. It differs from P. proteus in having a smooth lateral face without a carina <strong>and</strong> having a more open basal cavity which lacks <strong>the</strong> distinctive so-called paroistodiform character. The material from <strong>the</strong> Emanuel Formation is transitional between typical P. proteus from <strong>the</strong> late Tremadocian to Floian <strong>of</strong> Balto-Sc<strong>and</strong>ia <strong>and</strong> Paroistodus sp. from <strong>the</strong> Honghuayuan Formation <strong>of</strong> South China. It is comparable with P. proteus in having a prominent carina (Fig. 8A–E) or even a weak costa (Fig. 8J) on <strong>the</strong> lateral faces, but similar to Paroistodus sp. from <strong>the</strong> Honghuayuan Formation in lack <strong>of</strong> <strong>the</strong> paroistodiform feature. As mentioned above, absence <strong>of</strong> <strong>the</strong> paroistodiform character in species <strong>of</strong> Paroistodus co-occurring in <strong>the</strong> Emanuel Formation may indicate that this feature is caused by ecological adaption ra<strong>the</strong>r than as a phylogenetically Zhen & Nicoll: Canning Basin Serratognathus bilobatus Fauna 15 significant trait for Paroistodus. Interestingly, P. proteus from <strong>the</strong> Emanuel Formation <strong>of</strong> Western Australia <strong>and</strong> from <strong>the</strong> Latorp Limestone <strong>and</strong> Tøyen Shale <strong>of</strong> Sweden <strong>and</strong> Paroistodus sp. from <strong>the</strong> Honghuayuan Formation <strong>of</strong> South China come from three contrasting ecological/sedimentological settings; <strong>the</strong>y may represent three populations or subspecies <strong>of</strong> P. proteus. The typical latest Tremadocian <strong>and</strong> early Floian P. proteus-bearing successions in Sweden (e.g., Diabasbrottet area) were deposited in <strong>the</strong> outer shelf settings <strong>of</strong> <strong>the</strong> Cold Domain (Bergström et al., 2004), <strong>and</strong> <strong>the</strong> mid-upper part <strong>of</strong> <strong>the</strong> Emanuel Formation might be largely deposited in deep subtidal settings, while <strong>the</strong> Honghuayuan Formation with Paroistodus sp. apparently represents typical shallow subtidal environments. Therefore, in consideration <strong>of</strong> <strong>the</strong> relationship between <strong>the</strong>ir morphological variation <strong>and</strong> <strong>the</strong>ir ecological/geographical distributions, <strong>the</strong> material from <strong>the</strong> Emanuel Formation is considered as conspecific with type material <strong>of</strong> P. proteus, <strong>and</strong> Paroistodus sp. from <strong>the</strong> Honghuayuan Formation (Zhen et al., 2007b) might be better treated as a separate subspecies <strong>of</strong> P. proteus. Prioniodus P<strong>and</strong>er, 1856 Type species. Prioniodus elegans P<strong>and</strong>er, 1856. Prioniodus adami Stouge & Bagnoli, 1988 Fig. 6G–L Prioniodus sp. nov. C McTavish, 1973: 47, pl. 3, figs 4–6, ?11, 16, text-fig. 6f, g, i, ?j, k. Prioniodus adami Stouge & Bagnoli, 1988: 132, 133, pl. 11, figs 5–13 (cum syn.); ?Albanesi et al., 1998: 155, pl. 10, figs 1–3; Johnston & Barnes, 2000: 36, pl. 16, figs 9, 10, 13–16, 19; Pyle & Barnes, 2002: 110, pl. 26, figs 19–21. Material. Four specimens from two samples (Table 1). Remarks. Based on a large collection from Bed 9 <strong>of</strong> <strong>the</strong> Cow Head Group <strong>of</strong> western Newfoundl<strong>and</strong>, Stouge & Bagnoli (1988) established P. adami as having a septimembrate apparatus (pastinate Pa, <strong>and</strong> Pb, ramiform S <strong>and</strong> geniculate M elements), <strong>and</strong> also included in it <strong>the</strong> material from <strong>the</strong> Emanuel Formation that McTavish (1973), ascribed to Prioniodus sp. C except for <strong>the</strong> oistodiform element (his pl. 3, fig. 11, text-fig. 6j) which bears a short, adenticulate inner lateral process. Prioniodus adami is characterized by bearing small, closely-spaced denticles on <strong>the</strong> long posterior process <strong>of</strong> <strong>the</strong> S <strong>and</strong> P elements, as well as on <strong>the</strong> anterior <strong>and</strong> outer lateral processes <strong>of</strong> <strong>the</strong> P elements <strong>and</strong> <strong>the</strong> inner lateral process <strong>of</strong> <strong>the</strong> M element. The Pa element (Fig. 6G, H) from <strong>the</strong> Emanuel Formation is identical with those illustrated by McTavish (1973, pl. 3, figs 5, ?16), but exhibits less closely spaced denticles on <strong>the</strong> processes in comparison with <strong>the</strong> holotype (Stouge & Bagnoli, 1988, pl. 11, fig. 8). The M element from <strong>the</strong> Cow Head Group shows a long adenticulate outer lateral process <strong>and</strong> a long, denticulate inner lateral process with small, closely-spaced denticles, similar to those on <strong>the</strong> processes <strong>of</strong> <strong>the</strong> P <strong>and</strong> S elements, but no M element has been recovered from <strong>the</strong> samples <strong>of</strong> this study.